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Published on: July 21, 2021
Comparative genomics on BMP4 orthologs
1M&M Medical BioInformatics, Hongo 113-0033, Japan.
Abstract:
Bone morphogenetic proteins (BMPs) are implicated in cell-fate determination of embryonic stem (ES) cells and cancer cells. GREM1 (CKTSF1B1 or DAND2) and CER1 (Cerberus 1 or DAND4) are cysteine knot superfamily proteins, functioning as secreted-type BMP antagonists. BMP4 is preferentially expressed in diffuse-type gastric cancer cells. Here, vertebrate BMP4 orthologs were identified and characterized by using bioinformatics for comparative proteomics and comparative genomics analyses. Baboon BMP4 gene within AC153751.2 genome sequence encoded a 408-aa protein, showing A152V and S298P amino-acid substitutions compared with human BMP4. Cow Bmp4, bat Bmp4 and zebrafish bmp4 genes were located within AC149774.2, AC156788.2 and CR391996.2 genome sequences, respectively. Human BMP4 showed 99.5%, 98.0%, 97.8%, 97.1%, 96.3%, 83.3% and 71.1% total-amino-acid identity with baboon BMP4, cow Bmp4, bat Bmp4, mouse Bmp4, rat Bmp4, chicken bmp4 and zebrafish bmp4, respectively. Human BMP4 gene was found consisting of six exons, including novel exon 1C, and known exons 1 (1A or I), 1B (II), 2 (III), 3 (IV) and 4 (V). Forty human BMP4 ESTs started from exon 1, seven from intron 1 (5'-flanking region of exon 2), and two from exon 1C. Fourteen mouse Bmp4 ESTs started from exon 1, and one from intron 1. The 5'-flanking region of exon 1 and exon 1 itself, but not exons 1C and 1B, were well conserved between human BMP4 and rodent Bmp4 genes. The major promoter region of human BMP4 and rodent Bmp4 genes were located within the 5'-flanking region of exon 1. FOXA2, OLF1, and MYC-binding sites were conserved among the major promoter region of human, baboon, cow, bat, mouse and rat BMP4 orthologs.
Insights
Bone morphogenetic protein 4 (BMP4) orthologs were identified across vertebrates using bioinformatics. Key promoter regions and binding sites show conservation, suggesting functional importance in gene regulation.
Area of Science:
- Molecular Biology
- Genomics
- Bioinformatics
Background:
- Bone morphogenetic proteins (BMPs) play crucial roles in cell-fate determination in embryonic stem cells and cancer cells.
- BMP4 is notably expressed in diffuse-type gastric cancer cells.
- GREM1 and CER1 are secreted antagonists of BMP signaling.
Purpose of the Study:
- To identify and characterize vertebrate Bone morphogenetic protein 4 (BMP4) orthologs.
- To analyze comparative proteomics and genomics of BMP4 across species.
- To investigate the conservation of BMP4 gene structure and promoter regions.
Main Methods:
- Bioinformatic analysis was employed to identify and characterize BMP4 orthologs.
- Comparative proteomics and comparative genomics were utilized for analysis.
- Gene structure, exon-intron organization, and promoter regions were examined.
Main Results:
- Vertebrate BMP4 orthologs were identified in baboon, cow, bat, mouse, rat, chicken, and zebrafish.
- High amino acid identity was observed between human BMP4 and its orthologs, with notable variations in baboon BMP4.
- The 5'-flanking region of exon 1 and exon 1 itself are conserved in human and rodent BMP4, containing conserved transcription factor binding sites (FOXA2, OLF1, MYC).
Conclusions:
- Bioinformatic identification and characterization of BMP4 orthologs reveal significant conservation across vertebrates.
- Conserved promoter regions and transcription factor binding sites suggest a conserved regulatory mechanism for BMP4.
- These findings provide insights into the evolutionary and functional aspects of BMP4 in various species.
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